HGVS | Genome Assembly |
---|---|
NC_000011.10:g.299418T>G , CM000673.2:g.299418T>G | GRCh38 |
NC_000011.9:g.299418T>G , CM000673.1:g.299418T>G | GRCh37 |
NC_000011.8:g.289418T>G | NCBI36 |
NG_032892.1:g.5109A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382614.2:c.73A>C MANE Select | ENSP00000372059.2:p.Thr25Pro | |
NM_001025295.2:c.73A>C | NP_001020466.1:p.Thr25Pro | |
NM_001025295.3:c.73A>C MANE Select | NP_001020466.1:p.Thr25Pro |